Job Title: Quality Specialist Raw Material Disposition - Quality Raw Materials (GMP)

Reports To: Sr. Director, Raw Materials

Shifts: Day Shift, Monday-Friday, Core Hours 8:00am-5:30pm
Location: Redmond (Onsite)

The Role:
We are seeking a GMP focused Quality Specialist Raw Material Disposition to support GMP operations for late stage and commercial biologics manufacturing. In this role, you will be a key contributor to ensuring the quality, consistency, and regulatory compliance of raw materials across our Seattle and Redmond GMP facilities.

You will play a critical role in supplier and material onboarding, audit, complaint, and disposition activitiesin accordance withapproved proceduresll essential to our path toward commercialization.

This is a role for someone who is both scientifically sharp and operationally disciplined, who can think creatively while executing flawlessly in a regulated environment.

The Quality Specialist Raw Material Disposition will ensure compliance of all suppliers and raw materials dispositioned in support of our GMP manufacturing operations at the Seattle and Redmond, WA GMP facilities. These efforts support GMP manufacturing activities for biotherapeutic products.

What You9ll Do (GMP Heavy Responsibilities):

• Compile lot release documentation for Raw Materialdisposition.
• Ensure lot release deliverables are received from key stakeholders prior to Raw Materialdisposition.
• Support weekly lot disposition meeting with QA, Manufacturing, QC,etc.
• Review Deviations, OOS, and Change control records to ensure no impacttoProduct.
• Lead process improvements within Raw MaterialDisposition.
• Audit/inspection support for Raw MaterialDisposition asrequired.
• Partners with other QA peers to ensure consistency and efficiency within the QA department.
• Alert management of significant quality, compliance, supply, and safety risks.

Who You Are:

• Bachelor9s degree in biological or engineering scienceor equivalent work experience
• Minimum of 5 years relevant experience in a biopharmaceutical/Pharmaceutical cGMP manufacturing or similar environment.
• Ability to collaborate and communicate cross-functionally.
• Proven attention to detail

Why Join Us:

• Growth Opportunities: We9re a company that believes in continuous learning and development. Whether it9s professional courses, mentorship, or new projects, we9ll help you grow.
• Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. Site based role, Redmond.
• Inclusive Culture: We9re committed to building a diverse and inclusive environment where everyone9s voice is valued, and curiosity is encouraged.
• Innovative Projects: You9ll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.
• A Place for Big Ideas: We don9t just talk about thinking outside the boxwe throw the box away. If you9ve got ideas, we want to hear them.

Are You Still Curious?
If you9ve read this far, then chances are you9ve got a curious mind, just like us. So, what are you waiting for? Take the leap and apply today. We can9t wait to see where your curiosity leads you and how it will shape the future of Just Evotec Biologics.

Let your curiosity guide your career #BeCurious and explore the endless possibilities at Just Evotec Biologics!

The base pay range for this exempt position at commencement of employment is expected to be $87,000 to $95,000; Base salary offered may vary depending on individual9s skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits.